Results 161 to 170 of about 1,229,635 (199)

Moyamoya-like vasculopathy (moyamoya syndrome) in children

Child's Nervous System, 2004
A large variety of inherited or acquired childhood disorders and conditions may present in conjunction with progressive bilateral stenosis and/or occlusion of the terminal segments of the internal carotid artery. In addition, the development of pathological collateral vessels can be observed in the vicinity of the steno-occlusive changes in these ...
Peter, Horn, Stefan, Pfister, Eva, Bueltmann, Peter, Vajkoczy, Peter, Schmiedek   +4 more
openaire   +2 more sources

Moyamoya Disease (Moyamoya Syndrome) and Coarctation of the Aorta

Neuropediatrics, 2000
info:eu-repo/semantics ...
Christiaens, Florence, Van den Broeck, L K, Christophe, Catherine, Dan, Bernard   +3 more
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Moyamoya syndrome in a child with down syndrome

The Indian Journal of Pediatrics, 2005
Secondary Moyamoya disease, also known as Moyamoya syndrome has been rarely associated with Down syndrome. In pediatric patients, the usual presentation is that of ischemic stroke. Here is reported a 4-year-old child with Down syndrome and Moyamoya syndrome who presented with acute-onset right hemiplegia.
Utpal S, Bhalala, Pankaj R, Parekh
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Moyamoya Syndrome in a Child with Noonan Syndrome

Pediatric Neurology, 2011
Previous studies have rarely described the association between Noonan syndrome and moyamoya syndrome. Although most affected children with moyamoya exhibit ischemic symptoms, headache is also a frequent symptom. We report the case of a 9-year-old girl with Noonan syndrome and moyamoya syndrome that manifested as recurrent headaches without history of ...
Po-Cheng, Hung, Huei-Shyong, Wang, Alex M-C, Wong   +2 more
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Childhood Moyamoya Disease and Moyamoya Syndrome: A Pictorial Review

Pediatric Neurology, 2011
Moyamoya disease is an uncommon chronic cerebrovasculopathy, characterized by progressive stenosis of the terminal portion of the internal carotid artery and its main branches, in association with the development of compensatory collateral vessels at the base of the brain.
Stuart, Currie, Ashok, Raghavan, Ruth, Batty, Daniel J A, Connolly, Paul D, Griffiths   +4 more
openaire   +2 more sources

Moyamoya in a patient with Sneddon's syndrome

Clinical Neurology and Neurosurgery, 2015
NEUROFARBA Department, Neuroscience Section, University of Florence, Florence, Italy SOD Neurologia 2, Neuroscience Department, Azienda Ospedaliero Universitaria Careggi, Florence, Italy SOD Oculistica, Department of Translational Surgery and Medicine, Florence, Italy Department of Surgery and Translational Medicine, Division of Dermatology, University
FIERINI, FABIO, Barilaro, A, GIAMBENE, BARBARA, CARLUCCI, GIOVANNA, Grandi, V, MAIO, VINCENZA, PANTONI, LEONARDO   +6 more
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Moyamoya disease and down syndrome

The Indian Journal of Pediatrics, 2005
Moyamoya disease is an obstruction of the internal carotids and of the afferent and efferent channels of Willis polygon, which causes a collateral circulation, responsible for the typical angiographic image of a "puff of smoke" (Moyamoya, in Japanese). Its etiology is unknown, and it might be congenital or acquired.
Muferet, Erguven, Murat, Deveci, Tahsin, Turgut   +2 more
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[The moyamoya syndrome].

Zentralblatt fur Neurochirurgie, 1979
The Moyamoya vascular convolutions are interpreted as an unspecific collateral system in unilateral and bilateral progressive stenosing of the A. carotis interna and additional transdural externainterna anastomoses. In such cases one should speak of a Moyamoya syndrome. The designation Moyamoya disease only applies to the congenital form.
G, Gemende, K O, Kagel
openaire   +1 more source

Cardio-facio-cutaneous syndrome and moyamoya syndrome

Brain and Development, 2002
We reported a patient with cardio-facio-cutaneous (CFC) syndrome associated with moyamoya syndrome. The patient was referred at 6 years 5 months with left hemiplegia and right-sided eye deviation. He had an apparently short stature, macrocephaly, left ptosis and atopic skin, and was odd looking.
Yoshiko, Ishiguro, Tetsuo, Kubota, Junko, Takenaka, Koichi, Maruyama, Akihisa, Okumura, Tamiko, Negoro, Kazuyoshi, Watanabe   +6 more
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Seckel syndrome and moyamoya.

Journal of neurosurgery. Pediatrics, 2009
Seckel syndrome is an autosomal recessive disorder characterized by intrauterine and postnatal growth delay, microcephaly with mental retardation, and facial dysmorphisms including micrognathia, a recessed forehead, and a large beaked nose. Occurring in 1 in 10,000 children without sex preference, it is the most common primordial microcephalic ...
Patrick J, Codd, R Michael, Scott, Edward R, Smith   +2 more
openaire   +3 more sources